QA Engineer

• Provide Quality leadership as part of the New Modalities Quality team to ensure end to end quality oversight necessary to facilitate agility and speed-to-market while sustaining compliant supply of new modalities pipeline products to global markets.
• Stay ahead of current GMP requirements and industry trends as described in worldwide regulations and industry standards, and trend reporting.
• Maintain a subject matter expert level of knowledge related to these specialized areas of expertise, with a specific focus on Antibody Drug Conjugates.
• Provide guidance and coaching to manufacturing colleagues on new modalities quality oversight requirements and Health Authority GMP expectations.
• Evaluate current company and partner Quality Management Systems for seamless integration and realize synergies where available while ensuring compliance to GMP requirements.
• Ensure alignment to corporate policies as well as other divisional policies related to management of product quality.
• Implement a fit-for-purpose QMS, ensuring end-to-end quality oversight of new modalities products manufactured at our company and external partner sites.
• Partner with our company's Manufacturing Division QMS team for QMS updates as needed.
• Work in partnership across the organization (Research, Manufacturing and Commercial) to understand the unique requirements for the new modality products and ensure that these requirements are addressed via fit-for-purpose quality management oversight.
• Evaluate external partner Quality and compliance robustness and identify Quality risks.
• Work with internal colleagues and external partners to remediate risks as appropriate.
• Ensure that facilities/processes are compliant and support approval of new modality regulatory filings.
• Maintain close working relationship with our research and manufacturing divisions' Quality departments and Technical CMC teams for end-to-end Quality oversight/support of new modalities products.
• Support development of and report quality metrics measuring operational effectiveness to appropriate research and manufacturing divisions' governance forums.
• Ensure continuous improvement to new modalities QMS to maintain GMP and Regulatory compliance.

Director, Quality Assurance – New Modalities, Antibody Drug Conjugate

Business Analyst

• Support the identification, delivery, and sustainment of country-level automation, analytics, and AI solutions
• Assist with business case preparation, data analysis, dashboard/report building, workflow documentation
• Build and maintain country dashboards and basic automations under supervision
• Produce routine operational reports and Key Performance Indicators (KPI) dashboards
• Ensure adherence to ICH GCP, Company policies, and local regulations in documentation

Business Analyst – Automation, Analytics, AI

Director

• Developing and executing the strategy, design, and implementation of business transformation journey for Animal Health manufacturing IT division
• Ensuring the GAHM IT organization operates effectively and efficiently
• Acting as Chief of Staff and trusted advisor to the GAHM IT Lead
• Working across the GAHM IT Manufacturing, Quality & Supply Chain value teams
• Delivering on a multi-year roadmap of transformative business initiatives
• Providing leadership and direction for innovative solutions and operational execution
• Driving talent strategy and execution

Director, IT Strategy – Execution

• Reporting directly to the Head of their assigned functional area and acting as a member of their Leadership Team.
• The Executive Director, Functional Area Geography Lead leads global geographic strategy and performance across assigned region/ geography.
• Responsible for translating functional area and Global Data Management and Standards (GDMS) strategic imperatives into region-specific priorities and plans.
• Partner with GDMS and Global Clinical Trial Operations (GCTO) leaders to drive global alignment, standardization, and transformation of data-management practices.
• Represent their function and geography network in GDMS Leadership Team forums, and ensure resource excellence, capability growth, and operational readiness worldwide.

Executive Director, Geo Lead – Global Capability Lead, Clinical Data Management Services

Project Manager

• Managing the Value and Implementation process, including projects of significant complexity; driving cross-functional teams and leading by influence to develop comprehensive strategies and ensure successful execution.
• Act as enterprise leaders by guiding teams through the creation, approval, and execution of integrated project plans appropriate to the project's phase of development and complexity.
• Building and maintaining project plans and critical project information in enterprise project management systems and databases.
• Using these tools to integrate activities across key team members, proactively identify risks, and ensure clear and effective communication with key team, management, and cross-departmental stakeholders.
• Leveraging relationships and networks to improve and enhance team dynamics; proactively identifying and removing obstacles to drive business results.
• Navigating our Company process and organizational norms to enable teams to understand corporate business requirements, thereby enabling decision-making.
• Leading key team meetings including creating thoughtful agendas, ensuring appropriate participation, contributing project management insights, and following up to ensure the team continues to make progress while holding others accountable.
• Participating in GPAM departmental initiatives and workstreams aimed at improving the way that we work and the way that we interact with one another as well as other departments.
• Improving business processes to find new efficiencies and connect people to the information that they need.
• Providing mentoring, coaching, and oversight to Specialist and Senior Specialist project managers working on common projects.
• Sharing lessons learned and best practices to impact the GPAM community positively.

Associate Director, Project Management – Value & Implementation

Marketing

• Focus on supporting launch brands
• Day-to-day responsibilities focus on brand building, creative development, communication strategies, and leading the development of core content (promotional and medical ed) for HCPs and HCCs aligned with the commercial strategy and desired customer experience for key global brands
• Strategic partner and Content Expert to Global Brand Team, ensuring strategy realization during launch lifecycle
• Leads core content creative execution efforts from briefing creation (Workfront), content development and management (tools/technology enhancements), Medical Legal Review (PRT) and compliant content accessibility & storage (DAM)
• Embraces and implements technology advances to drive further content creation efficiency
• Co-manage and provide oversight in day-to-day agency relationships specific to core content creation (timelines, consolidated direction, scope support)
• Partner with CA Agency Team for AOR escalations
• Consultative partner to development of Branding & Campaign Implementation Guidance ensuring brand consistency and standardization (supporting scalability)
• Collaborates to ensure ELMs/HHI have access to globally-developed core strategic content, tools and technology for seamless re-use; executes governance plans
• Manages content lifecycle during launch/post-launch period (global content renewals, updates, retirement)
• Model the Content Accelerator vision through rapid adoption of AI enhancements
• Consultant to Global Brand and Content Accelerator Teams providing input, guidance, updates and validation to operating model principles and structure

Associate Director, Marketing Communications/Channels

Research Scientist

• Provide strategic leadership for CDx development and commercialization
• Oversee execution of strategies in collaboration with cross-functional teams
• Develop and direct CDx/IVD strategic approaches
• Lead cross-functional CDx Teams for various assets/biomarkers
• Partner with internal stakeholders to develop CDx strategies
• Drive CDx partner/platform assessment and selection
• Serve as a subject matter expert within the company
• Participate in meetings with global regulatory agencies to provide CDx expertise
• Oversee transfer of assays from in-house efforts to Dx companies
• Evaluate relevant new technologies

Senior Principal Scientist – Senior Director, Companion Diagnostics

Clinical Research

• Planning and directing clinical research activities involving new or marketed Neuroscience Medicines.
• Managing the entire cycle of clinical development, including study design, initiation, execution, monitoring, analysis, regulatory reporting, publication, and presentation at national and international meetings.
• Providing internal scientific leadership for cross-functional areas supporting clinical trials.
• Interacting externally with key opinion leaders.
• Evaluating pre-clinical and translational work for the purpose of generating early clinical development plans and Investigational New Drug applications.
• Developing clinical development strategies for investigational or marketed Neuroscience drugs.
• Planning clinical trials based on these clinical development strategies.
• Monitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed Neuroscience drugs.
• Analyzing and summarizing clinical findings to support decisions regarding safety and efficacy, as well as new drug applications and clinical study reports.

Senior Principal Scientist, Clinical Research, Neuroscience

• Develop and communicate data-driven and actionable insights that drive greater customer and market understanding to inform launch & go-to market strategies and help meet in-line commercial objectives.
• Interface and collaborate with many teams, requiring strong communication skills.
• Lead an insight team consisting of functional teams across market research, data strategy, forecasting, resource effectiveness, measurement, marketing/sales operations, digital analytics, competitive insights and strategy.
• Develop the next generation of leaders within DHH (Digital Human Health).

Director, Oncology Business Insights – Analytics

Medical Director

• planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area
• manage the entire cycle of clinical development for their assigned studies including study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication
• Evaluating pre-clinical and translational work for generating early clinical development plans and Investigational New Drug applications
• Developing clinical development strategies for investigational or marketed Hematology drugs
• Planning clinical trials based on the clinical development strategy
• Medical oversight and overall conduct of ongoing or new clinical trials
• Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy
• Participating in internal and joint internal/external research project teams relevant to the development of new compounds
• Supporting business development assessments of external opportunities

Senior Clinical Director, Clinical Research, Hematology

• The Executive Director will manage and oversee the entire cycle of late-stage clinical development from Phase 2 to Phase 5, including development of program strategy and design, protocol authoring, initiation, execution, monitoring, analysis, regulatory reporting, publication, and presentation at national and international meetings.
• They will lead cross-functional product development teams that oversee program strategy and execution, will provide internal scientific leadership for cross-functional areas supporting clinical trials, and will interact externally with key scientific leaders.
• Evaluating pre-clinical and translational work for the purpose of generating early clinical development plans and Investigational New Drug (IND) applications.
• Developing clinical development strategies for investigational or marketed medicines that incorporate the latest scientific developments, regulatory requirements, the competitive landscape, and commercial considerations.
• Executing the clinical strategy, planning clinical trials (design, operational plans, settings), and leading the clinical subteam.
• Monitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed medicines.
• Leading cross-functional product development teams that oversee overall strategy and execution for investigational or marketed medicines.
• Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publications.
• Participation in internal and joint internal/external research project teams relevant to the development of new compounds, and the further study of marketed compounds.

Executive Director, Product Development Team Leader, Clinical Research, Hematology – Lymphoma

Sales

• Demonstrate advanced expertise in developing and communicating a clear, compelling value proposition for company products.
• Serve as the primary point of contact for assigned customers.
• Establish and maintain strong relationships with key decision‑makers and influencers.
• Analyze and interpret trends within a complex oncology purchasing and prescribing environment.

Oncology Sales Specialist

• Support the identification, delivery, and sustainment of country-level automation, analytics, and AI solutions that enhance clinical trial operations
• Assist with business case preparation, data analysis, dashboard/report building, workflow documentation, solution testing, training, and user support
• Ensure solutions are compliant, adopted, and continuously improved
• Support alignment and scalability for regional and global solutions
• Assist in compiling business cases, gathering requirements, mapping processes, and documenting user stories and acceptance criteria
• Conduct data exploration and prepare baseline metrics to define problem statements and expected benefits
• Build and maintain country dashboards and basic automations under supervision using approved platforms
• Produce routine operational reports and Key Performance Indicators (KPI) dashboards; maintain data definitions and refresh cadence
• Ensure adherence to ICH GCP, Company policies, and local regulations in documentation and solution usage
• Collaborate with country, regional and headquarters teams

Consultant

• Learn our dairy technology solutions in depth, including product features, data interpretation, and practical applications on farm
• Join senior colleagues on farm visits and support customers in using technology effectively in their daily operations
• Respond to customer questions related to product use and functionality, using CRM tools and established support processes
• Support new product launches and pilot projects through installations, training, and structured feedback collection
• Work with sales and customer success teams by providing technical input for customer discussions and solution support
• Take part in internal training programs, certifications, and knowledge-sharing activities to continuously develop your skills
• Accurately record customer interactions and collect feedback to help improve our products and services

Regional Technical Consultant

Account Manager

• manage the business relationship between our company and assigned customer accounts
• Establishing profitable product access within our company product strategy
• Optimizing Net Sales and Contract Performance across a portfolio of our company products
• Lead pull through efforts of contracted positions with account team
• Ensuring proper oversight and compliance with all our company policies and exercising appropriate financial stewardship
• appropriately addressing customer educational needs, interacting with multiple stakeholders within the assigned account to enhance our company business relationship with its customers.
• engaging senior Institutional Leadership and building trust and credibility with customers through strong interpersonal relationships

MSD

Director, Quality Assurance – New Modalities, Antibody Drug Conjugate

Business Analyst – Automation, Analytics, AI

Director, IT Strategy – Execution

Executive Director, Geo Lead – Global Capability Lead, Clinical Data Management Services

Associate Director, Project Management – Value & Implementation

Associate Director, Marketing Communications/Channels

Senior Principal Scientist – Senior Director, Companion Diagnostics

Senior Principal Scientist, Clinical Research, Neuroscience

Director, Oncology Business Insights – Analytics

Senior Clinical Director, Clinical Research, Hematology

Executive Director, Product Development Team Leader, Clinical Research, Hematology – Lymphoma

Oncology Sales Specialist

Business Analyst – Automation, Analytics, AI

Regional Technical Consultant

Integrated Account Leader